WO1998030232A1 - Procedes et compositions de prevention de maladies auto-immunes - Google Patents
Procedes et compositions de prevention de maladies auto-immunes Download PDFInfo
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- WO1998030232A1 WO1998030232A1 PCT/CA1998/000015 CA9800015W WO9830232A1 WO 1998030232 A1 WO1998030232 A1 WO 1998030232A1 CA 9800015 W CA9800015 W CA 9800015W WO 9830232 A1 WO9830232 A1 WO 9830232A1
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
- C07K16/2818—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against CD28 or CD152
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/177—Receptors; Cell surface antigens; Cell surface determinants
- A61K38/1774—Immunoglobulin superfamily (e.g. CD2, CD4, CD8, ICAM molecules, B7 molecules, Fc-receptors, MHC-molecules)
Definitions
- Truncated versions of monoclonal antibodies may also be produced by recombinant techniques in which plasmids are generated which express the desired monoclonal antibody fragment (s) in a suitable host. Antibodies specific for mutagenic epitopes can also be generated.
- compositions for the prevention of autoimmune diseases in mammals.
- IFN- ⁇ remained essentially unaltered in these mice.
- Committed autoreactive cells including Thl cells, may accumulate in pancreatic islets but the functions of IL-4 predominate to inhibit IFN- ⁇ mediated ⁇ cell damage.
- FACS analyses of the phenotype and surface expression of various cell adhesion molecules in anti- CD28 treated and control NOD mice at 8-25 weeks of age also indicated that anti-CD28 mAb treatment did not interfere with the migration of diabetogenic T cells to pancreatic islets (data not shown) .
- the levels of surface expression of LFA-1, L-selectin and CD44 on the surface of splenic T cells did not suffer significantly between untreated and anti-CD28 treated NOD mice.
- CTLL-2 cells 1.5 x 10 4
- Ct.4S cells 5 x 10 3
- Cell proliferation was assessed by addition of [ 3 H] -thymidine for 8 h prior to termination of culture, and [ 3 H] thymidine incorporation was determined as above.
- Anti-CD28 mAb also significantly enhanced the NOD, and to a lesser extent the BALB/c, anti-CD3-induced splenic T cell proliferative response (Figure IB) .
- NOD and BALB/c splenic T cells were less responsive to CD28 costimulation (in terms of fold increases) than thymocytes from these mice, consistent with the notion that primed and naive T cells have different requirements for costimulation. Whereas primed splenic T cells require only TCR engagement to proliferate and produce IL-2, naive thymocytes require at least one additional costimulatory signal for optimal proliferation.
- NOD and BALB/c thymocytes obtained from 8 week old mice were activated by plate bound anti-CD3 in the absence or presence of 1 ⁇ g/ml soluble anti-CD28 mAb (optimal concentration) .
- Culture supernatants were removed, diluted and assayed for their IL-2 and IL-4 content by stimulation of proliferation of the CTLL-2 and CT.4S T cell lines, respectively.
- the results are shown in Figure 1C and ID.
- the CTLL-2 cpm values of [ 3 H] thymidine incorporation for anti-CD3 activated NOD and BALC/c T cells represented by the highest supernatant dilution were 9,064 ⁇ 1,246 and 3,715 ⁇ 940, respectively.
- the results of triplicate cultures are expressed as the mean values ⁇ SD, and are representative of four different experiments.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Immunology (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Biochemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Gastroenterology & Hepatology (AREA)
- Animal Behavior & Ethology (AREA)
- Zoology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Cell Biology (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/341,407 US6841152B1 (en) | 1997-01-10 | 1998-01-12 | Methods for protecting against autoimmune diabetes |
EP98900502A EP1015016A1 (fr) | 1997-01-10 | 1998-01-12 | Procedes et compositions de prevention de maladies auto-immunes |
CA002276733A CA2276733A1 (fr) | 1997-01-10 | 1998-01-12 | Procedes et compositions de prevention de maladies auto-immunes |
AU55462/98A AU5546298A (en) | 1997-01-10 | 1998-01-12 | Methods and compositions for preventing autoimmune disease |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002194814A CA2194814A1 (fr) | 1997-01-10 | 1997-01-10 | Stimulation des cellules t protectrices pour prevenir les maladies auto-immunes |
CA2,194,814 | 1997-01-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1998030232A1 true WO1998030232A1 (fr) | 1998-07-16 |
Family
ID=4159630
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CA1998/000015 WO1998030232A1 (fr) | 1997-01-10 | 1998-01-12 | Procedes et compositions de prevention de maladies auto-immunes |
Country Status (5)
Country | Link |
---|---|
US (1) | US6841152B1 (fr) |
EP (1) | EP1015016A1 (fr) |
AU (1) | AU5546298A (fr) |
CA (1) | CA2194814A1 (fr) |
WO (1) | WO1998030232A1 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1125585A1 (fr) * | 1999-08-30 | 2001-08-22 | Japan Tobacco Inc. | Traitements de maladies immunitaires |
WO2003078468A2 (fr) * | 2002-03-13 | 2003-09-25 | Tegenero Ag | Utilisation d'une substance active se liant a cd28 pour la preparation d'une composition pharmaceutique |
US7531168B2 (en) | 2001-02-16 | 2009-05-12 | Genetics Institute Llc | Method for downmodulating immune response in type I diabetes |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0426644D0 (en) * | 2004-12-03 | 2005-01-05 | Univ Aberdeen | T-cell modulation |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1990005541A1 (fr) * | 1988-11-23 | 1990-05-31 | The Regents Of The University Of Michigan | Immunotherapie mettant en ×uvre la stimulation de la cd28 |
WO1992000092A1 (fr) * | 1990-07-02 | 1992-01-09 | Bristol-Myers Squibb Company | Ligand pour recepteur a cd28 sur des lymphocytes b et procedes |
WO1993019767A1 (fr) * | 1992-04-07 | 1993-10-14 | The Regents Of The University Of Michigan | Immunoregulation recourant a la voie d'acces du cd28 |
WO1994028912A1 (fr) * | 1993-06-10 | 1994-12-22 | The Regents Of The University Of Michigan | Immunosuppression recourant a la voie d'acces du cd28 |
WO1995003408A1 (fr) * | 1993-07-26 | 1995-02-02 | Dana-Farber Cancer Institute | B7-2: contre-recepteur de ctla4/cd28 |
WO1995005464A1 (fr) * | 1993-08-16 | 1995-02-23 | Arch Development Corporation | B7-2: contre recepteur de ctla4/cd28 |
WO1996014865A1 (fr) * | 1994-11-10 | 1996-05-23 | Repligen Corporation | Procedes d'inhibition de la reaction du greffon contre l'hote lors d'une greffe de moelle osseuse |
-
1997
- 1997-01-10 CA CA002194814A patent/CA2194814A1/fr not_active Abandoned
-
1998
- 1998-01-12 EP EP98900502A patent/EP1015016A1/fr not_active Withdrawn
- 1998-01-12 WO PCT/CA1998/000015 patent/WO1998030232A1/fr not_active Application Discontinuation
- 1998-01-12 AU AU55462/98A patent/AU5546298A/en not_active Abandoned
- 1998-01-12 US US09/341,407 patent/US6841152B1/en not_active Expired - Fee Related
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1990005541A1 (fr) * | 1988-11-23 | 1990-05-31 | The Regents Of The University Of Michigan | Immunotherapie mettant en ×uvre la stimulation de la cd28 |
WO1992000092A1 (fr) * | 1990-07-02 | 1992-01-09 | Bristol-Myers Squibb Company | Ligand pour recepteur a cd28 sur des lymphocytes b et procedes |
WO1993019767A1 (fr) * | 1992-04-07 | 1993-10-14 | The Regents Of The University Of Michigan | Immunoregulation recourant a la voie d'acces du cd28 |
WO1994028912A1 (fr) * | 1993-06-10 | 1994-12-22 | The Regents Of The University Of Michigan | Immunosuppression recourant a la voie d'acces du cd28 |
WO1995003408A1 (fr) * | 1993-07-26 | 1995-02-02 | Dana-Farber Cancer Institute | B7-2: contre-recepteur de ctla4/cd28 |
WO1995005464A1 (fr) * | 1993-08-16 | 1995-02-23 | Arch Development Corporation | B7-2: contre recepteur de ctla4/cd28 |
WO1996014865A1 (fr) * | 1994-11-10 | 1996-05-23 | Repligen Corporation | Procedes d'inhibition de la reaction du greffon contre l'hote lors d'une greffe de moelle osseuse |
Non-Patent Citations (2)
Title |
---|
CAMERON M.J. ET AL: "Cytokine- and costimulation-mediated therapy of IDDM", CRITICAL REVIEWS IN IMMUNOLOGY, vol. 17, no. 5-6, 1997, pages 537 - 544, XP002061663 * |
LENSCHOW D.J. ET AL: "CD28/B7 regulation of Th1 and Th2 subsets in the development of autoimmune diabetes", IMMUNITY, vol. 5, no. 3, 1996, pages 285 - 293, XP002061664 * |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1125585A1 (fr) * | 1999-08-30 | 2001-08-22 | Japan Tobacco Inc. | Traitements de maladies immunitaires |
EP1125585A4 (fr) * | 1999-08-30 | 2007-08-29 | Japan Tobacco Inc | Traitements de maladies immunitaires |
US7465445B2 (en) | 1999-08-30 | 2008-12-16 | Japan Tobacco Inc. | Methods of preventing or treating graft versus host reaction by administering an antibody or portion thereof that binds to AILIM |
US7998478B2 (en) | 1999-08-30 | 2011-08-16 | Japan Tobacco, Inc. | Pharmaceutical composition for treating immune diseases |
US7531168B2 (en) | 2001-02-16 | 2009-05-12 | Genetics Institute Llc | Method for downmodulating immune response in type I diabetes |
WO2003078468A2 (fr) * | 2002-03-13 | 2003-09-25 | Tegenero Ag | Utilisation d'une substance active se liant a cd28 pour la preparation d'une composition pharmaceutique |
WO2003078468A3 (fr) * | 2002-03-13 | 2004-02-12 | Tegenero Ag | Utilisation d'une substance active se liant a cd28 pour la preparation d'une composition pharmaceutique |
Also Published As
Publication number | Publication date |
---|---|
EP1015016A1 (fr) | 2000-07-05 |
CA2194814A1 (fr) | 1998-07-10 |
AU5546298A (en) | 1998-08-03 |
US6841152B1 (en) | 2005-01-11 |
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